✦ LIBER ✦

A newly identified exonic mutation of the WT1 gene in a patient with Denys-Drash syndrome

✍ Scribed by MASAHIKO TSUDA; TAKESHI SAKIYAMA; MISAO OWADA; YASUSHI CHIBA

Book ID: 115176858
Publisher: John Wiley and Sons
Year: 1996
Tongue: English
Weight: 225 KB
Volume: 38
Category: Article
ISSN: 1328-8067
DOI: 10.1111/j.1442-200x.1996.tb03483.x

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

WT1 mutations in patients with Denys-Dra

WT1 mutations in patients with Denys-Drash syndrome: a novel mutation in exon 8 and paternal allele origin

✍ Agneta Nordenskjöld; Eitan Friedman; Maria Anvret 📂 Article 📅 1994 🏛 Springer 🌐 English ⚖ 803 KB

Denys-Drash syndrome (DDS) is characterized by early onset nephropathy, pseudohermaphroditism in males and a high risk for developing Wilm's tumour (WT). The exact cause of DDS is unknown but germline mutations in the Wilm's tumour suppressor gene (WT1) have recently been described in the majority o

Novel WT1 exon 9 mutation (D396Y) in a p

Novel WT1 exon 9 mutation (D396Y) in a patient with early onset Denys Drash syndrome

✍ Melissa Little; Gregory Carman; Eric Donaldson 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 12 KB 👁 2 views

AWT1exon 1 mutation in a child diagnosed

AWT1exon 1 mutation in a child diagnosed with Denys-Drash syndrome

✍ Suzanne Little; Sandra Hanks; Linda King-Underwood; Sue Picton; Catherine Cullin 📂 Article 📅 2004 🏛 Springer 🌐 English ⚖ 217 KB

Novel WT1 mutation (C388Y) in a female c

Novel WT1 mutation (C388Y) in a female child with Denys-Drash syndrome

✍ Swiatecka-Urban, Agnieszka; Mokrzycki, Michele H.; Kaskel, Frederick; Da Silva, 📂 Article 📅 2001 🏛 Springer 🌐 English ⚖ 33 KB

A NOVEL MISSENSE MUTATION OF THE WT1 GEN

A NOVEL MISSENSE MUTATION OF THE WT1 GENE CAUSING DENYS-DRASH SYNDROME WITH EXCEPTIONALLY MILD RENAL MANIFESTATIONS

✍ OHTA, SHOICHIRO; OZAWA, TETSUO; IZUMINO, KIYOSHI; SAKURAGAWA, NOBUO; FUSE, HIDEK 📂 Article 📅 2000 🏛 Lippincott Williams and Wilkins 🌐 English ⚖ 285 KB

A novel mutation ofWT1exon 9 in a patien

A novel mutation ofWT1exon 9 in a patient with Denys-Drash syndrome and pyloric stenosis

✍ Min Hu; Jonathon Craig; Neville Howard; Alex Kan; Jeffrey Chaitow; Dianne Little 📂 Article 📅 2004 🏛 Springer 🌐 English ⚖ 241 KB